Pure Global

PENTAX Medical Video Processor - Indonesia BPOM Medical Device Registration

PENTAX Medical Video Processor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801220366. The device is manufactured by PLEXUS MANUFACTURING SDN. BHD from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
PENTAX Medical Video Processor
Analysis ID: AKL 20801220366

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. INDOMEDIK NIAGA PERKASA

AR Address

JALAN RAYA KEBAYORAN LAMA NO.35 RT.008 RW.001 Kel. Sukabumi Selatan Kec, Kebon Jeruk, Jakarta Barat, provinsi DKI Jakarta

Registration Date

Feb 19, 2024

Expiry Date

Jun 12, 2026

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing